Evidence map›Paper›PMID 37408677›Full record

ArticleAdvances in radiation oncology

Proton Therapy for Unresectable and Medically Inoperable Locally Advanced Pancreatic Cancer: Results From a Multi-Institutional Prospective Registry.

Jacob Eckstein, J Isabelle Choi, Alicia Lozano, Nitin Ohri, Robert Press, Shaakir Hasan, Rafi Kabarriti, John Chang, James Urbanic, Michael Durci and 10 more

Open access · goldAbstract read
In one paragraph

Article in Advances in radiation oncology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.2field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 13 institutions in 1 country.

Jacob EcksteinNorthwell Health, Department of Radiation Medicine, New Hyde Park, New York.
J Isabelle ChoiNew York Proton Center, New York, New York.
Alicia LozanoNew York Proton Center, New York, New York.
Nitin OhriMontefiore Einstein Cancer Center, Department of Radiation Oncology, Bronx, New York.
Robert PressNew York Proton Center, New York, New York.
Shaakir HasanNew York Proton Center, New York, New York.
Rafi KabarritiMontefiore Einstein Cancer Center, Department of Radiation Oncology, Bronx, New York.
John ChangOklahoma Proton Center, Oklahoma City, Oklahoma.
James UrbanicUniversity of California, Department of Radiation Medicine and Applied Sciences, San Diego, California.
Michael DurciWillis Knighton Cancer Center, Shreveport, Louisiana.
Nasiruddin MohammedNorthwestern Medicine, Department of Radiation Oncology, Chicago, Illinois.
Craig StevensOakland University William Beaumont School of Medicine, Department of Radiation Oncology, Royal Oak, Michigan.
Henry TsaiPrinceton Radiation Oncology, Somerset, New Jersey.
Smith ApisarnthanaraxUniversity of Washington Medicine, Department of Radiation Oncology, Seattle, Washington.
William RegineUniversity of Maryland School of Medicine, Department of Radiation Oncology, Baltimore, Maryland.
Carlos VargasMayo Clinic, Department of Radiation Oncology, Rochester, Minnesota.
Romaine NicholsUniversity of Florida Protons, Department of Radiation Oncology, Gainesville, Florida.
Joseph HermanNorthwell Health, Department of Radiation Medicine, New Hyde Park, New York.
Charles B SimoneNew York Proton Center, New York, New York.
Arpit ChhabraNew York Proton Center, New York, New York.
New York Proton Center · USMontefiore Medical Center · USNorthwell Health · USMayo Clinic · USNorthwestern Medicine · USOakland University · USOklahoma Blood Institute · USSomerset Medical Center · USUniversity of California System · USUniversity of Florida Health · USUniversity of Maryland, Baltimore · USUniversity of Washington · USWillis-Knighton Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Compared with photon-based techniques, proton beam radiation therapy (PBT) may improve the therapeutic ratio of radiation therapy (RT) for locally advanced pancreatic cancer (LAPC), but available data have been limited to single-institutional experiences. This study examined the toxicity, survival, and disease control rates among patients enrolled in a multi-institutional prospective registry study and treated with PBT for LAPC. Methods and Materials: Between March 2013 and November 2019, 19 patients with inoperable disease across 7 institutions underwent PBT with definitive intent for LAPC. Patients received a median radiation dose/fractionation of 54 Gy/30 fractions (range, 50.4-60.0 Gy/19-33 fractions). Most received prior (68.4%) or concurrent (78.9%) chemotherapy. Patients were assessed prospectively for toxicities using National Cancer Institute Common Terminology Criteria for Adverse Events, version 4.0. Kaplan-Meier analysis was used to analyze overall survival, locoregional recurrence-free survival, time to locoregional recurrence, distant metastasis-free survival, and time to new progression or metastasis for the adenocarcinoma cohort (17 patients). Results: No patients experienced grade ≥3 acute or chronic treatment-related adverse events. Grade 1 and 2 adverse events occurred in 78.7% and 21.3% of patients, respectively. Median overall survival, locoregional recurrence-free survival, distant metastasis-free survival, and time to new progression or metastasis were 14.6, 11.0, 11.0, and 13.9 months, respectively. Freedom from locoregional recurrence at 2 years was 81.7%. All patients completed treatment with one requiring a RT break for stent placement. Conclusions: Proton beam RT for LAPC offered excellent tolerability while still maintaining disease control and survival rates comparable with dose-escalated photon-based RT. These findings are consistent with the known physical and dosimetric advantages offered by proton therapy, but the conclusions are limited owing to the patient sample size. Further clinical studies incorporating dose-escalated PBT are warranted to evaluate whether these dosimetric advantages translate into clinically meaningful benefits.

Identifiers

PMID37408677
PMCPMC10318270
OpenAlexW4366778790

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.